62791-22-4

Basic information

• Product Name: Silane, (1-cyclohexen-1-yloxy)(1,1-dimethylethyl)dimethyl-
• CAS NO: 62791-22-4
• Molecular Formula: C12H24OSi
• Molecular Weight: 212.407
• Mol File: 62791-22-4.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: Silane, (1-cyclohexen-1-yloxy)(1,1-dimethylethyl)dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, (1-cyclohexen-1-yloxy)(1,1-dimethylethyl)dimethyl-(62791-22-4)
• EPA Substance Registry System: Silane, (1-cyclohexen-1-yloxy)(1,1-dimethylethyl)dimethyl-(62791-22-4)

Safety Data

• Hazardous Substances Data: 62791-22-4(Hazardous Substances Data)

Upstream product

• 127375-61-5 (Bicyclo[3.1.0]hex-1-yloxy)-tert-butyl-dimethyl-silane 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 50984-16-2 rac-2-(phenylseleno)cyclohexanone 
• 930-68-7 cyclohexenone 
• 29681-57-0 tert-butyldimethylsilane 
• 108-94-1 cyclohexanone 
• 79184-90-0 tert-Butyl-dimethyl-(2-phenylselanyl-cyclohex-1-enyloxy)-silane 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 77086-38-5 ketene t-butyldimethylsilyl methyl acetal 

Downstream Products

• 130751-69-8 2-[Benzo[1,3]dioxol-5-yl-(tert-butyl-dimethyl-silanyloxy)-methyl]-cyclohexanone 
• 130751-69-8 2-[Benzo[1,3]dioxol-5-yl-(tert-butyl-dimethyl-silanyloxy)-methyl]-cyclohexanone 
• 233257-09-5 (2S)-2-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]cyclohexanone 
• 681146-44-1 (1R,6S,8R)-1-(tert-butyldimethylsiloxy)-8-[(1R,2S,5R)-2-(1-methyl-1-phenylethyl)-5-methylcyclohexyloxycarbonyl]bicyclo[4.2.0]octane 
• 681146-47-4 (1S,6R,8R)-1-(tert-butyldimethylsiloxy)-8-[(1R,2S,5R)-2-(1-methyl-1-phenylethyl)-5-methylcyclohexyloxycarbonyl]bicyclo[4.2.0]octane 
• 657428-65-4 (1RS,6SR,8RS)-1-hydroxy-8-hydroxymethylbicyclo[4.2.0]octane 
• 657428-65-4 (1RS,6SR,8SR)-1-hydroxy-8-hydroxymethylbicyclo[4.2.0]octane 
• 68614-38-0 2-(2'-nitrophenyl)cyclohexanone 

Relevant articles and documents

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Chiral Zinc(II)-Catalyzed Enantioselective Tandem α-Alkenyl Addition/Proton Shift Reaction of Silyl Enol Ethers with Ketimines

A new catalytic asymmetric tandem α-alkenyl addition/proton shift reaction of silyl enol ethers with ketimines was serendipitously discovered in the presence of chiral N,N′-dioxide/ZnII complexes. The proton shift preferentially proceeded inste

Synthesis of Functionalized Medium-Sized trans-Cycloalkenes by 4π Electrocyclic Ring Opening/Alkylation Sequence

Development of a novel synthetic method for medium-sized trans-cycloalkenes (TCAs) is described. Functionalized TCAs are readily prepared from simple cycloalkanones in a few steps, namely, enol silyl ether formation, [2+2] cycloaddition, and domino 4π ele

Unprecedented alkylation of silicon enolates with alcohols via carbenium ion formations catalyzed by tin hydroxide-embedded montmorillonite

The solid acid, tin hydroxide-embedded montmorillonite, catalyzes the unprecedented alkylation of various silicon enolates with primary, secondary and tertiary benzylic alcohols as well as secondary allylic alcohols. The acid catalysis of Sn-Mont was not only higher than that of the other ion-exchanged montmorillonites (M-Mont; M?=?H, Ti, Fe and Al), but also higher than that of the typical homogeneous acid catalysts such as BF3·OEt2, TMSOTf and TfOH.